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Klinische Monatsblatter Fur Augenheilkunde
|
August 14, 2010
[Implantation of multifocal add-on IOLs simultaneously with cataract surgery: results of a prospective study]
M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde
|
December 17, 2008
[Correction of aphakia with retroiridally fixated IOL]
M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde
|
December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]
C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]
C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology
|
November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings
C Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Klinische Monatsblatter Fur Augenheilkunde
|
August 14, 2010
[Implantation of multifocal add-on IOLs simultaneously with cataract surgery: results of a prospective study]
M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde
|
December 17, 2008
[Correction of aphakia with retroiridally fixated IOL]
M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde
|
December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]
C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]
C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology
|
November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings
C Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
Page
of 1